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Phenotype and genotype predictors of BMI variability among European adults

BACKGROUND/OBJECTIVE: Obesity is a complex and multifactorial disease resulting from the interactions among genetics, metabolic, behavioral, sociocultural and environmental factors. In this sense, the aim of the present study was to identify phenotype and genotype variables that could be relevant de...

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Autores principales: Goni, Leticia, García-Granero, Marta, Milagro, Fermín I., Cuervo, Marta, Martínez, J. Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966508/
https://www.ncbi.nlm.nih.gov/pubmed/29795275
http://dx.doi.org/10.1038/s41387-018-0041-1
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author Goni, Leticia
García-Granero, Marta
Milagro, Fermín I.
Cuervo, Marta
Martínez, J. Alfredo
author_facet Goni, Leticia
García-Granero, Marta
Milagro, Fermín I.
Cuervo, Marta
Martínez, J. Alfredo
author_sort Goni, Leticia
collection PubMed
description BACKGROUND/OBJECTIVE: Obesity is a complex and multifactorial disease resulting from the interactions among genetics, metabolic, behavioral, sociocultural and environmental factors. In this sense, the aim of the present study was to identify phenotype and genotype variables that could be relevant determinants of body mass index (BMI) variability. SUBJECTS/METHODS: In the present study, a total of 1050 subjects (798 females; 76%) were included. Least angle regression (LARS) analysis was used as regression model selection technique, where the dependent variable was BMI and the independent variables were age, sex, energy intake, physical activity level, and 16 polymorphisms previously related to obesity and lipid metabolism. RESULTS: The LARS analysis obtained the following formula for BMI explanation: (64.7 + 0.10 × age [years] + 0.42 × gender [0, men; 1, women] + −40.6 × physical activity [physical activity level] + 0.004 × energy intake [kcal] + 0.74 × rs9939609 [0 or 1–2 risk alleles] + −0.72 × rs1800206 [0 or 1–2 risk alleles] + −0.86 × rs1801282 [0 or 1–2 risk alleles] + 0.87 × rs429358 [0 or 1–2 risk alleles]. The multivariable regression model accounted for 21% of the phenotypic variance in BMI. The regression model was internally validated by the bootstrap method (r(2) original data set = 0.208, mean r(2) bootstrap data sets = 0.210). CONCLUSION: In conclusion, age, physical activity, energy intake and polymorphisms in FTO, APOE, PPARG and PPARA genes are significant predictors of the BMI trait.
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spelling pubmed-59665082018-05-24 Phenotype and genotype predictors of BMI variability among European adults Goni, Leticia García-Granero, Marta Milagro, Fermín I. Cuervo, Marta Martínez, J. Alfredo Nutr Diabetes Article BACKGROUND/OBJECTIVE: Obesity is a complex and multifactorial disease resulting from the interactions among genetics, metabolic, behavioral, sociocultural and environmental factors. In this sense, the aim of the present study was to identify phenotype and genotype variables that could be relevant determinants of body mass index (BMI) variability. SUBJECTS/METHODS: In the present study, a total of 1050 subjects (798 females; 76%) were included. Least angle regression (LARS) analysis was used as regression model selection technique, where the dependent variable was BMI and the independent variables were age, sex, energy intake, physical activity level, and 16 polymorphisms previously related to obesity and lipid metabolism. RESULTS: The LARS analysis obtained the following formula for BMI explanation: (64.7 + 0.10 × age [years] + 0.42 × gender [0, men; 1, women] + −40.6 × physical activity [physical activity level] + 0.004 × energy intake [kcal] + 0.74 × rs9939609 [0 or 1–2 risk alleles] + −0.72 × rs1800206 [0 or 1–2 risk alleles] + −0.86 × rs1801282 [0 or 1–2 risk alleles] + 0.87 × rs429358 [0 or 1–2 risk alleles]. The multivariable regression model accounted for 21% of the phenotypic variance in BMI. The regression model was internally validated by the bootstrap method (r(2) original data set = 0.208, mean r(2) bootstrap data sets = 0.210). CONCLUSION: In conclusion, age, physical activity, energy intake and polymorphisms in FTO, APOE, PPARG and PPARA genes are significant predictors of the BMI trait. Nature Publishing Group UK 2018-05-24 /pmc/articles/PMC5966508/ /pubmed/29795275 http://dx.doi.org/10.1038/s41387-018-0041-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Goni, Leticia
García-Granero, Marta
Milagro, Fermín I.
Cuervo, Marta
Martínez, J. Alfredo
Phenotype and genotype predictors of BMI variability among European adults
title Phenotype and genotype predictors of BMI variability among European adults
title_full Phenotype and genotype predictors of BMI variability among European adults
title_fullStr Phenotype and genotype predictors of BMI variability among European adults
title_full_unstemmed Phenotype and genotype predictors of BMI variability among European adults
title_short Phenotype and genotype predictors of BMI variability among European adults
title_sort phenotype and genotype predictors of bmi variability among european adults
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966508/
https://www.ncbi.nlm.nih.gov/pubmed/29795275
http://dx.doi.org/10.1038/s41387-018-0041-1
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